相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Mammalian nuclear TRUB1, mitochondrial TRUB2, and cytoplasmic PUS10 produce conserved pseudouridine 55 in different sets of tRNA
Shaoni Mukhopadhyay et al.
RNA (2021)
Human GTPBP5 is involved in the late stage of mitoribosome large subunit assembly
Miriam Cipullo et al.
NUCLEIC ACIDS RESEARCH (2021)
Roe of GTPases in Driving Mitoribosome Assembly
Priyanka Maiti et al.
TRENDS IN CELL BIOLOGY (2021)
Mitochondrial Kinases and the Role of Mitochondrial Protein Phosphorylation in Health and Disease
Veronika Kotrasova et al.
LIFE-BASEL (2021)
FASTKD2 promotes cancer cell progression through upregulating Myc expression in pancreatic ductal adenocarcinoma
Rui Fang et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2020)
Mouse Trmt2B protein is a dual specific mitochondrial metyltransferase responsible for m5U formation in both tRNA and rRNA
Ivan Laptev et al.
RNA BIOLOGY (2020)
Identification of key genes involved in the development and progression of early-onset colorectal cancer by co-expression network analysis
Xiaoqiong Mo et al.
ONCOLOGY LETTERS (2020)
A report of gonadal mosaicism inDHX30-related neurodevelopmental disorder
Laura A. Cross et al.
CLINICAL DYSMORPHOLOGY (2020)
Mutations in FASTKD2 are associated with mitochondrial disease with multi-OXPHOS deficiency
Wei Xiujuan et al.
HUMAN MUTATION (2020)
TRMT2B is responsible for both tRNA and rRNA m5U-methylation in human mitochondria
Christopher A. Powell et al.
RNA BIOLOGY (2020)
The human mitochondrial 12S rRNA m4C methyltransferase METTL15 is required for mitochondrial function
Hao Chen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2020)
YBEY is an essential biogenesis factor for mitochondrial ribosomes
Sabrina Summer et al.
NUCLEIC ACIDS RESEARCH (2020)
Methylation of Ribosomal RNA: A Mitochondrial Perspective
M. Isabel G. Lopez Sanchez et al.
FRONTIERS IN GENETICS (2020)
Structural Insights into the Mechanism of Mitoribosomal Large Subunit Biogenesis
Mateusz Jaskolowski et al.
MOLECULAR CELL (2020)
A homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assembly
Michela Di Nottia et al.
NEUROBIOLOGY OF DISEASE (2020)
Human GTPBP5 (MTG2) fuels mitoribosome large subunit maturation by facilitating 16S rRNA methylation
Priyanka Maiti et al.
NUCLEIC ACIDS RESEARCH (2020)
Distinct pre-initiation steps in human mitochondrial translation
Anas Khawaja et al.
NATURE COMMUNICATIONS (2020)
RCC1L (WBSCR16) isoforms coordinate mitochondrial ribosome assembly through their interaction with GTPases
Aurelio Reyes et al.
PLOS GENETICS (2020)
Leigh Syndrome in a Pedigree Harboring the m.1555A>G Mutation in the Mitochondrial 12S rRNA
Mouna Habbane et al.
GENES (2020)
Dual function of GTPBP6 in biogenesis and recycling of human mitochondrial ribosomes
Elena Lavdovskaia et al.
NUCLEIC ACIDS RESEARCH (2020)
Elongational stalling activates mitoribosome-associated quality control
Nirupa Desai et al.
SCIENCE (2020)
Structure of the mature kinetoplastids mitoribosome and insights into its large subunit biogenesis
Heddy Soufari et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
Novel role of mitochondrial GTPases 1 in pathological cardiac hypertrophy
Dachun Xu et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2019)
MRPS25 mutations impair mitochondrial translation and cause encephalomyopathy
Enrico Bugiardini et al.
HUMAN MOLECULAR GENETICS (2019)
NDUFAB1 confers cardio-protection by enhancing mitochondrial bioenergetics through coordination of respiratory complex and supercomplex assembly
Tingting Hou et al.
CELL RESEARCH (2019)
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
Jonathan P. Bradfield et al.
HUMAN MOLECULAR GENETICS (2019)
Structural insights into dimethylation of 12S rRNA by TFB1M: indispensable role in translation of mitochondrial genes and mitochondrial function
Xiaodan Liu et al.
NUCLEIC ACIDS RESEARCH (2019)
Mettl17, a regulator of mitochondrial ribosomal RNA modifications, is required for the translation of mitochondrial coding genes
Zhennan Shi et al.
FASEB JOURNAL (2019)
NDUFAB1 protects against obesity and insulin resistance by enhancing mitochondrial metabolism
Rufeng Zhang et al.
FASEB JOURNAL (2019)
Structural consequences of the interaction of RbgA with a 50S ribosomal subunit assembly intermediate
Amal Seffouh et al.
NUCLEIC ACIDS RESEARCH (2019)
METTL15 introduces N4-methylcytidine into human mitochondrial 12S rRNA and is required for mitoribosome biogenesis
Lindsey Van Haute et al.
NUCLEIC ACIDS RESEARCH (2019)
Mitoribosomal small subunit biogenesis in trypanosomes involves an extensive assembly machinery
Martin Saurer et al.
SCIENCE (2019)
Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects
Chih-Ping Chen et al.
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY (2019)
MitoRibo-Tag Mice Provide a Tool for In Vivo Studies of Mitoribosome Composition
Jakob D. Busch et al.
CELL REPORTS (2019)
Structural modules of the stress-induced protein HflX: an outlook on its evolution and biological role
Krishnamoorthi Srinivasan et al.
CURRENT GENETICS (2019)
Mitochondrial acyl carrier protein (ACP) at the interface of metabolic state sensing and mitochondrial function
Ali J. Masud et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2019)
A variant in MRPS14 (uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement
Christopher B. Jackson et al.
HUMAN MOLECULAR GENETICS (2019)
Mutations in the MRPS28 gene encoding the small mitoribosomal subunit protein bS1m in a patient with intrauterine growth retardation, craniofacial dysmorphism and multisystemic involvement
Juliette Pulman et al.
HUMAN MOLECULAR GENETICS (2019)
Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome
Nurun Nahar Borna et al.
NEUROGENETICS (2019)
MTERFD1 promotes cell growth and irradiation resistance in colorectal cancer by upregulating interleukin-6 and interleukin-11
Xiaoshuang Liu et al.
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES (2019)
Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies
Thatjana Gardeitchik et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
A Large-Scale, Exome-Wide Association Study of Han Chinese Women Identifies Three Novel Loci Predisposing to Breast Cancer
Bo Zhang et al.
CANCER RESEARCH (2018)
Mitochondrial transcription and translation: overview
Aaron R. D'Souza et al.
MITOCHONDRIAL DISEASES (2018)
Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency
Anlu Chen et al.
HUMAN MOLECULAR GENETICS (2018)
MTG1 couples mitoribosome large subunit assembly with intersubunit bridge formation
Hyun-Jung Kim et al.
NUCLEIC ACIDS RESEARCH (2018)
The MRPS18-2 protein levels correlate with prostate tumor progression and it induces CXCR4-dependent migration of cancer cells
Muhammad Mushtaq et al.
SCIENTIFIC REPORTS (2018)
Kinetics and Mechanism of Mammalian Mitochondrial Ribosome Assembly
Daniel F. Bogenhagen et al.
CELL REPORTS (2018)
ACP Acylation Is an Acetyl-CoA-Dependent Modification Required for Electron Transport Chain Assembly
Jonathan G. Van Vranken et al.
MOLECULAR CELL (2018)
Unique features of mammalian mitochondrial translation initiation revealed by cryo-EM
Eva Kummer et al.
NATURE (2018)
The human Obg protein GTPBP10 is involved in mitoribosomal biogenesis
Elena Lavdovskaia et al.
NUCLEIC ACIDS RESEARCH (2018)
Human GTPBP10 is required for mitoribosome maturation
Priyanka Maiti et al.
NUCLEIC ACIDS RESEARCH (2018)
A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability
Hana Antonicka et al.
EMBO REPORTS (2017)
A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome
Iliana A. Chatzispyrou et al.
HUMAN MOLECULAR GENETICS (2017)
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome
Caterina Garone et al.
HUMAN MOLECULAR GENETICS (2017)
The Pseudouridine Synthase RPUSD4 Is an Essential Component of Mitochondrial RNA Granules
Sofia Zaganelli et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2017)
MiR-542-3p exerts tumor suppressive functions in non-small cell lung cancer cells by upregulating FTSJ2
Bin Liu et al.
LIFE SCIENCES (2017)
Mitochondrial mutations in 12S rRNA and 16S rRNA presenting as chronic progressive external ophthalmoplegia (CPEO) plus A case report
Zhan-Yun Lv et al.
MEDICINE (2017)
Identification of FASTKD2 compound heterozygous mutations as the underlying cause of autosomal recessive MELAS-like syndrome
Da Hye Yoo et al.
MITOCHONDRION (2017)
Structures of the human mitochondrial ribosome in native states of assembly
Alan Brown et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2017)
The FASTK family of proteins: emerging regulators of mitochondrial RNA biology
Alexis A. Jourdain et al.
NUCLEIC ACIDS RESEARCH (2017)
Evidence for rRNA 2′-O-methylation plasticity: Control of intrinsic translational capabilities of human ribosomes
Jenny Erales et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
Dynamical differential networks and modules inferring disrupted genes associated with the progression of Alzheimer's disease
Zhengling Wang et al.
EXPERIMENTAL AND THERAPEUTIC MEDICINE (2017)
Structures of the human mitochondrial ribosome in native states of assembly
Alan Brown et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2017)
WBSCR16 Is a Guanine Nucleotide Exchange Factor Important for Mitochondrial Fusion
Guorui Huang et al.
CELL REPORTS (2017)
Lessons learned from additional research analyses of unsolved clinical exome cases
Mohammad K. Eldomery et al.
GENOME MEDICINE (2017)
Distinct RNA-unwinding mechanisms of DEAD-box and DEAH-box RNA helicase proteins in remodeling structured RNAs and RNPs
Benjamin Gilman et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2017)
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
Davor Lessel et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome
Nicole J. Lake et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
The human RNA-binding protein RBFA promotes the maturation of the mitochondrial ribosome
Agata Rozanska et al.
BIOCHEMICAL JOURNAL (2017)
An emerging role for the ribosome as a nexus for post-translational modifications
Deniz Simsek et al.
CURRENT OPINION IN CELL BIOLOGY (2017)
Fyn kinase regulates translation in mammalian mitochondria
Emine C. Koc et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS (2017)
C21orf57 is a human homologue of bacterial YbeY proteins
Anubrata Ghosal et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2017)
A Genome-wide CRISPR Death Screen Identifies Genes Essential for Oxidative Phosphorylation
Jason D. Arroyo et al.
Cell Metabolism (2016)
CLPP coordinates mitoribosomal assembly through the regulation of ERAL1 levels
Karolina Szczepanowska et al.
EMBO JOURNAL (2016)
YphC and YsxC GTPases assist the maturation of the central protuberance, GTPase associated region and functional core of the 50S ribosomal subunit
Xiaodan Ni et al.
NUCLEIC ACIDS RESEARCH (2016)
The conserved GTPase HflX is a ribosome splitting factor that binds to the E-site of the bacterial ribosome
Mackenzie L. Coatham et al.
NUCLEIC ACIDS RESEARCH (2016)
Human mitochondrial ribosomes can switch their structural RNA composition
Joanna Rorbach et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2016)
Mechanisms and Dynamics of Protein Acetylation in Mitochondria
Josue Baeza et al.
TRENDS IN BIOCHEMICAL SCIENCES (2016)
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Fergus J. Couch et al.
NATURE COMMUNICATIONS (2016)
Integrative radiogenomic analysis for multicentric radiophenotype in glioblastoma
Doo-Sik Kong et al.
ONCOTARGET (2016)
Identification and validation of regulatory SNPs that modulate transcription factor chromatin binding and gene expression in prostate cancer
Hong-Jian Jin et al.
ONCOTARGET (2016)
Hierarchical RNA Processing Is Required for Mitochondrial Ribosome Assembly
Oliver Rackham et al.
CELL REPORTS (2016)
Mitochondrial 16S rRNA Is Methylated by tRNA Methyltransferase TRMT61B in All Vertebrates
Dan Bar-Yaacov et al.
PLOS BIOLOGY (2016)
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies
Masakazu Kohda et al.
PLOS GENETICS (2016)
The mitochondrial acyl carrier protein (ACP) coordinates mitochondrial fatty acid synthesis with iron sulfur cluster biogenesis
Jonathan G. Van Vranken et al.
ELIFE (2016)
Trransiating the Genome in Time and Space: Specialized Ribosomes, RNA. Regulons, and RNA-Binding Proteins
Zhen Shi et al.
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 31 (2015)
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia
Minal J. Menezes et al.
HUMAN MOLECULAR GENETICS (2015)
The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease
Joanna L. Elson et al.
MITOCHONDRION (2015)
HflX is a ribosome-splitting factor rescuing stalled ribosomes under stress conditions
Yanqing Zhang et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2015)
Alzheimer's disease is associated with altered expression of genes involved in immune response and mitochondrial processes in astrocytes
Shobana Sekar et al.
NEUROBIOLOGY OF AGING (2015)
MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities
Fabian Baertling et al.
NEUROGENETICS (2015)
MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathy
Felix Distelmaier et al.
NEUROGENETICS (2015)
FASTKD2 is an RNA-binding protein required for mitochondrial RNA processing and translation
Johannes Popow et al.
RNA (2015)
The complete structure of the 55S mammalian mitochondrial ribosome
Basil J. Greber et al.
SCIENCE (2015)
The structure of the human mitochondrial ribosome
Alexey Amunts et al.
SCIENCE (2015)
HflX is a ribosome-splitting factor rescuing stalled ribosomes under stress conditions
Yanqing Zhang et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2015)
The Human Mitochondrial DEAD-Box Protein DDX28 Resides in RNA Granules and Functions in Mitoribosome Assembly
Ya-Ting Tu et al.
CELL REPORTS (2015)
Mitochondrial RNA Granules Are Centers for Posttranscriptional RNA Processing and Ribosome Biogenesis
Hana Antonicka et al.
CELL REPORTS (2015)
Mitochondrial m.1584A 12S m26A rRNA methylation in families with m.1555A>G associated hearing loss
Mary O'Sullivan et al.
HUMAN MOLECULAR GENETICS (2015)
Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis
Sukanya Horpaopan et al.
INTERNATIONAL JOURNAL OF CANCER (2015)
Initial Steps in RNA Processing and Ribosome Assembly Occur at Mitochondrial DNA Nucleoids
Daniel F. Bogenhagen et al.
CELL METABOLISM (2014)
A new system for naming ribosomal proteins
Nenad Ban et al.
CURRENT OPINION IN STRUCTURAL BIOLOGY (2014)
Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes
Vladimir V. Sharoyko et al.
HUMAN MOLECULAR GENETICS (2014)
Assignment of 2′-O-Methyltransferases to Modification Sites on the Mammalian Mitochondrial Large Subunit 16 S Ribosomal RNA (rRNA)
Ken-Wing Lee et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
The novel mitochondrial 16S rRNA 2336T>C mutation is associated with hypertrophic cardiomyopathy
Zhong Liu et al.
JOURNAL OF MEDICAL GENETICS (2014)
Phenotypic diversity associated with the MT-TV gene m.1644G > A mutation, a matter of quantity
Matthew J. Fraidakis et al.
MITOCHONDRION (2014)
MRM2 and MRM3 are involved in biogenesis of the large subunit of the mitochondrial ribosome
Joanna Rorbach et al.
MOLECULAR BIOLOGY OF THE CELL (2014)
The complete structure of the large subunit of the mammalian mitochondrial ribosome
Basil J. Greber et al.
NATURE (2014)
Architecture of mammalian respiratory complex I
Kutti R. Vinothkumar et al.
NATURE (2014)
Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families
Gerald Egger et al.
NEUROGENETICS (2014)
Functional domains of the 50S subunit mature late in the assembly process
Ahmad Jomaa et al.
NUCLEIC ACIDS RESEARCH (2014)
MPV17L2 is required for ribosome assembly in mitochondria
Ilaria Dalla Rosa et al.
NUCLEIC ACIDS RESEARCH (2014)
Genome-Wide and Gene-Based Association Studies of Anxiety Disorders in European and African American Samples
Takeshi Otowa et al.
PLOS ONE (2014)
Structure of the large ribosomal subunit from human mitochondria
Alan Brown et al.
SCIENCE (2014)
Structural and Functional Insights into the Mode of Action of a Universally Conserved Obg GTPase
Boya Feng et al.
PLOS BIOLOGY (2014)
NSUN4 Is a Dual Function Mitochondrial Protein Required for Both Methylation of 12S rRNA and Coordination of Mitoribosomal Assembly
Metodi Dimitrov Metodiev et al.
PLOS GENETICS (2014)
De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boywith psychomotor retardation and dysmorphic features
Konstantinos Varvagiannis et al.
META GENE (2014)
A de novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features
A. Dheedene et al.
MOLECULAR SYNDROMOLOGY (2014)
Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency
Valerie Serre et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2013)
Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy
Christopher J. Carroll et al.
JOURNAL OF MEDICAL GENETICS (2013)
The conserved interaction of C7orf30 with MRPL14 promotes biogenesis of the mitochondrial large ribosomal subunit and mitochondrial translation
Stephen Fung et al.
MOLECULAR BIOLOGY OF THE CELL (2013)
Conserved Bacterial RNase YbeY Plays Key Roles in 70S Ribosome Quality Control and 16S rRNA Maturation
Asha Ivy Jacob et al.
MOLECULAR CELL (2013)
Human G-proteins, ObgH1 and Mtg1, associate with the large mitochondrial ribosome subunit and are involved in translation and assembly of respiratory complexes
Tetsuya Kotani et al.
NUCLEIC ACIDS RESEARCH (2013)
MTERF3 Regulates Mitochondrial Ribosome Biogenesis in Invertebrates and Mammals
Anna Wredenberg et al.
PLOS GENETICS (2013)
Regulation of mammalian mitochondrial translation by post-translational modifications
Emine C. Koc et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS (2012)
C7orf30 specifically associates with the large subunit of the mitochondrial ribosome and is involved in translation
Bas F. J. Wanschers et al.
NUCLEIC ACIDS RESEARCH (2012)
C7orf30 is necessary for biogenesis of the large subunit of the mitochondrial ribosome
Joanna Rorbach et al.
NUCLEIC ACIDS RESEARCH (2012)
Human C4orf14 interacts with the mitochondrial nucleoid and is involved in the biogenesis of the small mitochondrial ribosomal subunit
J. He et al.
NUCLEIC ACIDS RESEARCH (2012)
cis-Expression QTL Analysis of Established Colorectal Cancer Risk Variants in Colon Tumors and Adjacent Normal Tissue
Lenora W. M. Loo et al.
PLOS ONE (2012)
Structure of the human MTERF4-NSUN4 protein complex that regulates mitochondrial ribosome biogenesis
Henrik Spahr et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Trmt61B is a methyltransferase responsible for 1-methyladenosine at position 58 of human mitochondrial tRNAs
Takeshi Chujo et al.
RNA (2012)
Structure of the Essential MTERF4:NSUN4 Protein Complex Reveals How an MTERF Protein Collaborates to Facilitate rRNA Modification
Elena Yakubovskaya et al.
STRUCTURE (2012)
De Novo Deletion of Chromosome 20q13.33 in a Patient with Tracheo-esophageal Fistula, Cardiac Defects and Genitourinary Anomalies Implicates GTPBP5 as a Candidate Gene
Benjamin D. Solomon et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2011)
RNA processing in human mitochondria
Maria I. G. Lopez Sanchez et al.
CELL CYCLE (2011)
A Common Variant in TFB1M Is Associated with Reduced Insulin Secretion and Increased Future Risk of Type 2 Diabetes
Thomas Koeck et al.
CELL METABOLISM (2011)
MTERF4 Regulates Translation by Targeting the Methyltransferase NSUN4 to the Mammalian Mitochondrial Ribosome
Yolanda Camara et al.
CELL METABOLISM (2011)
Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy
Paulien Smits et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
Exome Sequencing Identifies MRPL3 Mutation in Mitochondrial Cardiomyopathy
Louise Galmiche et al.
HUMAN MUTATION (2011)
NOA1 is an essential GTPase required for mitochondrial protein synthesis
Mateusz Kolanczyk et al.
MOLECULAR BIOLOGY OF THE CELL (2011)
Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunit
Sven Dennerlein et al.
BIOCHEMICAL JOURNAL (2010)
Human mitochondrial mRNAs-like members of all families, similar but different
Richard J. Temperley et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2010)
Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene
Emna Mkaouar-Rebai et al.
BIOSCIENCE REPORTS (2010)
NAD+-dependent Deacetylase SIRT3 Regulates Mitochondrial Protein Synthesis by Deacetylation of the Ribosomal Protein MRPL10
Yongjie Yang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss
Jianxin Lu et al.
MITOCHONDRION (2010)
Role of Escherichia coli YbeY, a highly conserved protein, in rRNA processing
Bryan W. Davies et al.
MOLECULAR MICROBIOLOGY (2010)
ERAL1 is associated with mitochondrial ribosome and elimination of ERAL1 leads to mitochondrial dysfunction and growth retardation
Takeshi Uchiumi et al.
NUCLEIC ACIDS RESEARCH (2010)
Methylation of 12S rRNA Is Necessary for In Vivo Stability of the Small Subunit of the Mammalian Mitochondrial Ribosome
Metodi D. Metodiev et al.
CELL METABOLISM (2009)
Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNAVal causing MNGIE-like gastrointestinal dysmotility and cachexia
Rita Horvath et al.
JOURNAL OF NEUROLOGY (2009)
FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency
Daniele Ghezzi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
New polymorphic mtDNA restriction site in the 12S rRNA gene detected in Tunisian patients with non-syndromic hearing loss
Emna Mkaouar-Rebai et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2008)
Integrative genomic and gene expression analysis of chromosome 7 identified novel oncogene loci in non-small cell lung cancer
Jennifer M. Campbell et al.
GENOME (2008)
A novel tRNAVal mitochondrial DNA mutation causing MELAS
Kurenal Tanji et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2008)
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation
A. Saada et al.
JOURNAL OF MEDICAL GENETICS (2007)
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip
Marianne Leveque et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2007)
A novel mutation 3090 G > A of the mitochondrial 16S ribosomal RNA associated with myopathy
L. Coulbault et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2007)
Dysregulation of X-linked gene expression in Klinefelter's syndrome and association with verbal cognition
Marquis P. Vawter et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2007)
Role of GTPases in ribosome assembly
Katrin Karbstein
BIOPOLYMERS (2007)
MTERF3 is a negative regulator of mammalian mtDNA transcription
Chan Bae Park et al.
CELL (2007)
Human small G proteins, ObgH1, and ObgH2, participate in the maintenance of mitochondria and nucleolar architectures
Yasuhiro Hirano et al.
GENES TO CELLS (2006)
Evidence for an early gene duplication event in the evolution of the mitochondrial transcription factor B family and maintenance of rRNA methyltransferase activity in human mtTFB1 and mtTFB2
Justin Cotney et al.
JOURNAL OF MOLECULAR EVOLUTION (2006)
The Escherichia coli GTPase CgtAE is involved in late steps of large ribosome assembly
Mengxi Jiang et al.
JOURNAL OF BACTERIOLOGY (2006)
Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment
E Ballana et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
A small protein unique to bacteria organizes rRNA tertiary structure over an extensive region of the 50 S ribosomal subunit
C Maeder et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss
ZY Li et al.
HUMAN GENETICS (2005)
Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large chinese family with maternally inherited hearing loss
RH Li et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2004)
Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss
R Li et al.
JOURNAL OF MEDICAL GENETICS (2004)
Differentially expressed genes in pancreatic ductal adenocarcinomas identified through serial analysis of gene expression
SR Hustinx et al.
CANCER BIOLOGY & THERAPY (2004)
Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large chinese family
H Zhao et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation
C Miller et al.
ANNALS OF NEUROLOGY (2004)
Childhood neurological presentation of a novel mitochondrial tRNAVal gene mutation
EL Blakely et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2004)
Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation
Y Bykhovskaya et al.
MOLECULAR GENETICS AND METABOLISM (2004)
Differentially expressed genes in sporadic amyotrophic lateral sclerosis spinal cords - screening by molecular indexing and subsequent cDNA microarray analysis
S Ishigaki et al.
FEBS LETTERS (2002)
Transcriptional regulation of cortical neuron migration by POU domain factors
RJ McEvilly et al.
SCIENCE (2002)
Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation
R McFarland et al.
NATURE GENETICS (2002)
A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy
RH Hsieh et al.
JOURNAL OF BIOMEDICAL SCIENCE (2001)
分享论文
